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38384-43-9

3,6-Dimethyl-4,5-dihydroxy-octadien-(2,6) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 38384-43-9 Structure

  • Basic information

    1. Product Name: 3,6-Dimethyl-4,5-dihydroxy-octadien-(2,6)
    2. Synonyms:
    3. CAS NO:38384-43-9
    4. Molecular Formula:
    5. Molecular Weight: 170.252
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 38384-43-9.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3,6-Dimethyl-4,5-dihydroxy-octadien-(2,6)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,6-Dimethyl-4,5-dihydroxy-octadien-(2,6)(38384-43-9)
    11. EPA Substance Registry System: 3,6-Dimethyl-4,5-dihydroxy-octadien-(2,6)(38384-43-9)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 38384-43-9(Hazardous Substances Data)

38384-43-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38384-43-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,3,8 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38384-43:
(7*3)+(6*8)+(5*3)+(4*8)+(3*4)+(2*4)+(1*3)=139
139 % 10 = 9
So 38384-43-9 is a valid CAS Registry Number.

38384-43-9Upstream product

38384-43-9Downstream Products

38384-43-9Relevant articles and documents

Simple and expeditious pinacol coupling of non usual α,β-unsaturated carbonyl compounds in water

Billamboz, Muriel,Sotto, Nicolas,Chevrin-Villette, Carole,Len, Christophe

, p. 46026 - 46030 (2015)

Using zinc (0) in a 5% v AcOH aqueous solution allowed the efficient pinacol coupling of aliphatic or aromatic unusual, α,β-unsaturated carbonyl compounds such as citral A in good to excellent yields (56-99%). It can also be successfully applied to acetophenone.

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